n14162025
| type | n |
| lex_filenum | 26 |
| def | a disease caused by a dominant mutant gene on an autosome |
| Outgoing links | |
| Hypernym | genetic disease, genetic disorder, genetic abnormality, genetic defect, congenital disease, inherited disease, inherited disorder, hereditary disease, hereditary condition |
| Hyponym | Huntington's chorea, Huntington's disease; malignant hyperthermia; Marfan's syndrome; neurofibromatosis, von Recklinghausen's disease; osteogenesis imperfecta |
| Incoming links | |
| Hyponym | genetic disease, genetic disorder, genetic abnormality, genetic defect, congenital disease, inherited disease, inherited disorder, hereditary disease, hereditary condition |
| Hypernym | Huntington's chorea, Huntington's disease; malignant hyperthermia; Marfan's syndrome; neurofibromatosis, von Recklinghausen's disease; osteogenesis imperfecta |
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